The Amyotrophic Lateral Sclerosis Functional Rating Scale: Difference between revisions

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= '''The Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS)''' =
<div class="editorbox">
'''Original Editor '''- [[User:Ajay Upadhyay|Ajay Upadhyay]]


== <br>Objective ==
'''Top Contributors''' - {{Special:Contributors/{{FULLPAGENAME}}}} &nbsp;
</div>  


<br>Its an instrument for assessing the activities of daily living of patients with Amyotrophic Lateral Sclerosis. Its also used to record disease progression in patients with ALS against other functional scales, quantitative isometric muscle testing, and global assessment scales.
= '''The Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS)'''  =


== Intended Population ==
== <br>Objective  ==


<br>All the patients with amyotrophic lateral sclerosis.
<br>Its an instrument for assessing the activities of daily living of patients with Amyotrophic Lateral Sclerosis. Its also used to record disease progression in patients with ALS against other functional scales, quantitative isometric muscle testing, and global assessment scales.  


== Intended Population  ==


<br>All the patients with amyotrophic lateral sclerosis.


== Method of Use ==
<br>


<br>It consist of 10 items of functional rating scale which includes activities of daily living, speech, salivation, and swallowing. Each item is scored from 0 to 4. 4 is given if person is normal, and 0 for poor performance<br>
== Method of Use  ==


#Following items are included in the assessment scale-
<br>It consist of 10 items of functional rating scale which includes activities of daily living, speech, salivation, and swallowing. Each item is scored from 0 to 4. 4 is given if person is normal, and 0 for poor performance<br>
 
#Following items are included in the assessment scale-  
#1. Speech  
#1. Speech  
#2. Salivation  
#2. Salivation  
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== <br>Interpretation:  ==
== <br>Interpretation:  ==


<br>minimum score: 0 <br>maximum score: 40 <br>The higher the score the more function is retained.
<br>minimum score: 0 <br>maximum score: 40 <br>The higher the score the more function is retained.  
 


<br>


== Reliability ==
== Reliability ==


=== <br>Test-retest Reliability ===
=== <br>Test-retest Reliability ===


<br>It shows'''test-retest reliability''' (ICC = 0.95) and is consistent.
<br>It shows'''test-retest reliability''' (ICC = 0.95) and is consistent.  


<br><u>'''Interrater/Intrarater Reliability'''</u><br>Kaufmann et al, 2007<br>• Excellent interrater reliability when administered by a primary rater; (ICC = 0.93)<br>• Excellent interrater reliability when administered by a back-up rater, n = 9 (ICC = 0.93)<br>• Excellent intrarater reliability, n = 41 (ICC = 0.95)<br>• Excellent reliability when test is administered on telephone, n = 27 (ICC = 0.97)  
<br><u>'''Interrater/Intrarater Reliability'''</u><br>Kaufmann et al, 2007<br>• Excellent interrater reliability when administered by a primary rater; (ICC = 0.93)<br>• Excellent interrater reliability when administered by a back-up rater, n = 9 (ICC = 0.93)<br>• Excellent intrarater reliability, n = 41 (ICC = 0.95)<br>• Excellent reliability when test is administered on telephone, n = 27 (ICC = 0.97)  


== <br>Validity ==
== <br>Validity ==


=== <br>Criterion Validity  ===
=== <br>Criterion Validity  ===


<br>''Brooks, B., Sanjak, M., et al. (1996)''. "The amyotrophic lateral sclerosis functional rating scale-Assessment of activities of daily living in patients with amyotrophic lateral sclerosis." Archives of Neurology 53(2): 141-147.
<br>''Brooks, B., Sanjak, M., et al. (1996)''. "The amyotrophic lateral sclerosis functional rating scale-Assessment of activities of daily living in patients with amyotrophic lateral sclerosis." Archives of Neurology 53(2): 141-147.  


<br>The '''sensitivity '''of ALSFRS scores to change in 53 patients’ statuses over time was assessed in this two phased trial. The ALSFRS scores declined together in motor and pulmonary function indicating its sensitivity to change.<br><br>
<br>The '''sensitivity '''of ALSFRS scores to change in 53 patients’ statuses over time was assessed in this two phased trial. The ALSFRS scores declined together in motor and pulmonary function indicating its sensitivity to change.<br><br>

Revision as of 17:47, 28 January 2015

Original Editor - Ajay Upadhyay

Top Contributors - Ajay Upadhyay and Amrita Patro  

The Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS)[edit | edit source]


Objective
[edit | edit source]


Its an instrument for assessing the activities of daily living of patients with Amyotrophic Lateral Sclerosis. Its also used to record disease progression in patients with ALS against other functional scales, quantitative isometric muscle testing, and global assessment scales.

Intended Population[edit | edit source]


All the patients with amyotrophic lateral sclerosis.


Method of Use[edit | edit source]


It consist of 10 items of functional rating scale which includes activities of daily living, speech, salivation, and swallowing. Each item is scored from 0 to 4. 4 is given if person is normal, and 0 for poor performance

  1. Following items are included in the assessment scale-
  2. 1. Speech
  3. 2. Salivation
  4. 3. Swallowing
  5. 4. Handwriting
  6. 5. Cutting food and handling utensils (with or without gastrostomy)
  7. 6. Dressing and hygiene
  8. 7. Turning in bed and adjusting bed clothes
  9. 8. Walking
  10. 9. Climbing stairs
  11. 10. Breathing


Interpretation:
[edit | edit source]


minimum score: 0
maximum score: 40
The higher the score the more function is retained.


Reliability[edit | edit source]


Test-retest Reliability
[edit | edit source]


It showstest-retest reliability (ICC = 0.95) and is consistent.


Interrater/Intrarater Reliability
Kaufmann et al, 2007
• Excellent interrater reliability when administered by a primary rater; (ICC = 0.93)
• Excellent interrater reliability when administered by a back-up rater, n = 9 (ICC = 0.93)
• Excellent intrarater reliability, n = 41 (ICC = 0.95)
• Excellent reliability when test is administered on telephone, n = 27 (ICC = 0.97)


Validity
[edit | edit source]


Criterion Validity
[edit | edit source]


Brooks, B., Sanjak, M., et al. (1996). "The amyotrophic lateral sclerosis functional rating scale-Assessment of activities of daily living in patients with amyotrophic lateral sclerosis." Archives of Neurology 53(2): 141-147.


The sensitivity of ALSFRS scores to change in 53 patients’ statuses over time was assessed in this two phased trial. The ALSFRS scores declined together in motor and pulmonary function indicating its sensitivity to change.